Recombinant KAT enzyme and process for its preparation

ABSTRACT

Disclosed are isolated DNAs encoding a kynurenine aminotransferase selected from the group consisting of: 
     (a) isolated DNA sequences which encode rat KAT; 
     (b) an isolated DNA sequence which hybridizes to isolated DNA sequences of (a) above and which encodes a mammalian KAT enzyme; and 
     (c) an isolated DNA sequence differing from the isolated DNA sequences of (a) and (b) above in codon sequence due to the degeneracy of the genetic code, and which encodes a KAT enzyme. 
     Vectors and host cells containing the same, oligonucleotide probes for identifying kynurenine aminotransferase, and isolated and purified kynurenine aminotransferase are also disclosed.

This is a continuation in part of Ser. No. 08/271,667 filed Jul. 7, 1994 now U.S. Pat. No. 5,817,496.

FIELD OF THE INVENTION

The present invention relates to DNA sequences that code for kynurenine aminotransferase.

BACKGROUND OF THE INVENTION

The enzyme kynurenine aminotransferase (known in the art as KAT) catalyzes the biosynthesis of kynurenic acid (KYNA) from kynurenine (KYN) and is singularly responsible for the regulation of extracellular KYNA concentrations in the brain (J. Neurochem., 57:533-540 (1991)).

KYNA is an effective excitatory amino acid (EAA) receptor antagonist with a particularly high affinity to the glycine modulatory site of the N-methyl-D-aspartate (NMDA) receptor complex (J. Neurochem., 52:1319-1328 (1989)). As a naturally occurring brain metabolite (J. Neurochem., 51:177-180 (1988); and Brain Res., 454:164-169 (1988)), KYNA probably serves as a negative endogenous modulator of cerebral glutamatergic function (Ann. N.Y. Acad. Sci., 648:140-153 (1992)).

EAA receptors and in particular NMDA receptors are known to play a central role in the function of the mammalian brain (Watkins et al, In: The NMDA Receptor, page 242, (1989), Eds., Oxford University Press, Oxford). For example, NMDA receptor activation is essential for cognitive processes, such as, for example, learning and memory (Watkins et al, In: The NMDA Receptor, Eds., pages 137-151, (1989), Oxford University press, Oxford) and for brain development (Trends Pharmacol. Sci., 11:290-296 (1990)).

It follows that a reduction in NMDA receptor function will have detrimental consequences for brain physiology and, consequently, for the entire organism. For example, the decline in the number of NMDA receptors which occurs in the aged brain (Synapse, 6:343-388 (1990)) is likely associated with age-related disorders of cognitive functions.

In the brain, KYNA concentrations and the activity of KYNA's biosynthetic enzyme KAT show a remarkable increase with age (Brain Res., 558:1-5, (1992); and Neurosci. Lett., 94:145-150 (1988)). KAT inhibitors, by providing an increase of the glutamatergic tone at the NMDA receptor, could therefore be particularly useful in situations where NMDA receptor function is insufficient and/or KAT activity and KYNA levels are abnormally enhanced. Hence they could be particularly useful in the treatment of the pathological consequences associated with the aging processes in the brain which are, for example, cognitive disorders including, e.g., attention and memory deficits and vigilance impairments in the elderly.

KAT inhibitors may also be useful in the treatment of perinatal brain disorders which may be related to irregularities in the characteristic region specific pattern of postnatal KAT development (Baran et al, Dev. Brain Res., 74:283-286 (1993)).

In subcellular fractionation studies KAT activity was recovered in the cytosol and in mitochondria (J. Neurochem., supra).

Most nuclear-encoded precursors of mitochondrial proteins contain amino-terminal presequences (Pfanner et al, In: Current Topics in Bioenergetics, 15:177-219 (1987); Lee Ed., New York Academic Press; and Nicholson et al, In: Protein Transfer and Organelle Biogenesis, Das and Robins Eds., New York Academic Press (1988)). These presequences are required for the precursor to enter the mitochondrial matrix, where they are proteolytically removed (Hurt et al, FEBS Lett., 178:306 (1984); Horwich et al, EMBO J., 4:1129 (1985). This cleavage is not essential for completing import but is necessary for further assembly of the newly imported polypeptides into functional complexes (Zwizinski et al, J. Biol. Chem., 258:13340 (1983); Lewin et al, J. Biol. Chem., 258:6750 (1983); Ou et al, J. Biochem., 100:1287 (1986)). Precursor targeting sequences differ considerably in their structures. One of the few common themes is the high content of positively charged amino acids and of hydroxylated amino acids. Presequences may form an amphipathic structure in the form of either α-helices or β-sheets (von Heijne et al, EMBO J., 5:1335 (1986); Roise et al, EMBO J., 5:1327 (1986); and Vassarotti et al, EMBO J., 6:705 (1987)). Despite the large variability of the sequences of mitochondrial leader peptides, relatively minor alterations of the presequence can prevent cleavage by the processing peptidase (Hurt et al, J. Biol. Chem., 262:1420 (1987)). This suggests that distinct, but up to now undefined, structural elements are required for cleavage. Similarly, the cleavage sites show wide variation among different precursors of a single organism and among precursors of different organisms.

Interestingly, using the protein algorithm described by Gavel et al (Protein Engineering, 4:33-37 (1990)), a potential mitochondrial transit peptide is predicted either in position 1 to 24 of the deduced protein of cDNA-2 and in position 1 to 44 of the deduced protein of cDNA-3 disclosed in the present invention (see FIGS. 3-4 and Example 3). Recently Perry et al (Mol. Pharm., 43:660-665 (1993)) reported the cloning of a cDNA coding for rat kidney cytosolic cysteine conjugate β-lyase.. When the cDNA was inserted into the expression vector PVS1000 and transfected into COS-1 tissue culture cells, a 7-10 fold increase in cytosolic β-lyase and glutamine transaminase K activities was detected. The deduced amino acid sequence of rat β-lyase is identical to the deduced amino acid sequence of cDNA-1 (rat KAT) except for two residues (see FIG. 2). Moreover the existence of cDNA-2 and cDNA-3 was not reported by Perry et al (Mol. Pharm., supra).

Even more recently Perry et al (FEBS Lett., 360:277-280 (1995)) reported the cloning of a cDNA for human kidney cysteine conjugate beta-lyase whose sequence is identical to the sequence of the human KAT described in the present patent application. Whereas the identity with cysteine conjugate β-lyase and glutamine transaminase K is well documented (Abraham et al, Analytical Biochem., 197:421-427 (1991)), there are no reports indicating identity of kynurenine transaminase with either β-lyase or glutamine transaminase K.

SUMMARY OF THE INVENTION

We now report the cloning of mammalian kynurenine aminotransferases.

A first aspect of the present invention relates to isolated DNA sequences encoding a KAT enzyme selected from the group consisting of: (a) isolated DNA sequences which encode rat KAT; (b) an isolated DNA sequence which hybridizes to isolated DNA sequences of (a) above and which encodes a mammalian KAT enzyme; and (c) an isolated DNA sequence differing from the isolated DNA sequences of (a) and (b) above in codon sequence due to the degeneracy of the genetic code, and which encodes a KAT enzyme.

A second aspect of the present invention relates to vectors comprising a cloned DNA sequence as given above.

A third aspect of the present invention are host cells transformed with a vector as given above.

A fourth aspect of the present invention is an oligonucleotide probe capable of selectively hybridizing to a DNA comprising a portion of a gene coding for a KAT enzyme.

A fifth aspect of the present invention is isolated and purified KAT enzyme which is coded for by a DNA sequence selected from the group consisting of: (a) isolated DNA sequences which encode rat KAT; (b) an isolated DNA sequence which hybridizes to an isolated DNA sequence of (a) above and which encodes a mammalian KAT enzyme; and (c) an isolated DNA sequence differing from the isolated DNA sequences of (a) and (b) above in codon sequence due to the degeneracy of the genetic code, and which encodes a KAT enzyme.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 Partial amino acid sequence of rat KAT: N-terminus of mature KAT (SEQ ID NO:14), a CNBr fragment (SEQ ID NO:15), tryptic fragment 112 of KAT (SEQ ID NO:16) and tryptic fragment 130 of KAT (SEQ ID NO:17).

FIGS. 2A-2C nucleotide sequence and deduced amino acid sequence of rat KAT (cDNA-1) (SEQ ID NO:18). The putative pyridoxal phosphate binding site, Ser--Ala--Gly--Lys--Ser--Phe, is underlined. Triplets differing from rat β-lyase cDNA (Perry et al, supra) are boxed.

FIGS. 3A-3D nucleotide sequence and deduced amino acid sequences of rat KAT (cDNA-2) (SEQ ID NO:19). Two proteins can be synthesized: one starting from nucleotide 619 and including a putative mitochondrial targeting peptide, the other beginning at the same ATG starting codon as in the case of cDNA-l. The putative pyridoxal phosphate binding site, Ser--Ala--Gly--Lys--Ser--Phe, is underlined. Triplets differing from rat β-lyase CDNA (Perry et al, supra) are boxed.

FIGS. 4A-4D nucleotide sequence and deduced amino acid sequences of rat KAT (cDNA-3) (SEQ ID NO:5). The sequence of cDNA-3 is identical to that of CDNA-1 except for an insertion of 208 base pairs in the 5'-untranslated region. The insertion creates an additional stretch of 34 amino acids in frame with the cDNA-1 deduced protein sequence. The insertion of these 208 base pairs occurs between nucleotide 237 and 238 of the cDNA-1 sequence.

FIGS. 5A and 5B cytosolic enzyme activities in transfected COS-1 cells: 5A, glutamine transaminase K activity; 5B, kynurenine transaminase activity. Sense: pSVL-KAT transfected COS-1 cells where cDNA-1 is in the sense orientation. Antisense: PSVL-KAT transfected COS-1 cells were cDNA-1 is in reverse orientation. Each value is the mean of three separate experiments.

FIG. 6 Partial amino acid sequence of human KAT I: tryptic fragments F11 (SEQ ID NO:2); F13 (SEQ ID NO:3); and F14 (SEQ ID NO:4) of the human KAT I.

FIGS. 7A-7C nucleotide sequence and deduced amino acid sequence of human KAT I (SEQ ID NO:1).

DETAILED DESCRIPTION OF THE INVENTION

Amino acid sequences disclosed herein are presented in the amino to carboxy direction, from left to right. The amino and carboxy groups are not presented in the sequence. Nucleotide sequences are presented herein by single strand only, in the 5' to 3' direction, from left to right. Nucleotides and amino acids are represented herein in the manner recommended by the IUPAC-IUB Biochemical Nomenclature Commission, or (for amino acids) by three letter code.

The kynurenine aminotransferase enzyme of the present invention includes proteins homologous to, and having essentially the same biological properties as, the protein coded for by the nucleotide sequences herein disclosed. This definition is intended to encompass natural allelic variants of KAT sequence.

Cloned genes of the present invention may code for KAT of any species of origin, but preferably code for enzymes of mammalian origin. Thus, DNA sequences which hybridize to the sequences given in FIGS. 2A-2C (SEQ ID NO:18), 3A-3D (SEQ ID NO:19), 4A-4D (SEQ ID NO:5) and 7A-7C (SEQ ID NO:1) and which code for expression of KAT are also an aspect of this invention. Conditions which will permit other DNA sequences which code for expression of KAT to hybridize to the sequences given in FIGS. 2A-2C (SEQ ID NO:18), 3A-3D (SEQ ID NO:19), 4A-4D (SEQ ID NO:5) and 7A-7C (SEQ ID NO:1) can be determined in a routine manner. Further, DNA sequences which code for polypeptides coded for by the sequences given in FIGS. 2A-2C (SEQ ID NO:18), 3A-3D (SEQ ID NO:19), 4A-4D (SEQ ID NO:5) and 7A-7C (SEQ ID NO:1) or sequences which hybridize thereto and code for a KAT enzyme, but which differ in codon sequence from these due to degeneracy of the genetic code, are also an aspect of this invention. The degeneracy of the genetic code, which allows different nucleic acid sequences to code for the same protein or peptide, is well known in the literature. See, e.g., Toole et al, U.S. Pat. No. 4,757,006 at column 2, Table 1.

DNA which encodes the KAT enzyme may be obtained by a variety of means well known to the expert in the art and disclosed by, for example, Maniatis et al, Molecular Cloning: A Laboratory Manual, 2nd Ed., Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1989).

For example, DNA which encodes the KAT enzyme may be obtained by screening of mRNA or genomic DNA with oligonucleotide probes generated from the KAT enzyme gene sequence information provided herein. Probes may be labeled with a detectable group such as a fluorescent group, a radioactive atom or a chemiluminescent group in accordance with known procedures and used in conventional hybridization assays, as described by, for example, Maniatis et al, supra.

KAT gene sequences may alternatively be recovered by use of the polymerase chain reaction (PCR) procedure, with the PCR oligonucleotide primers described herein or with oligonucleotide primers being produced from the KAT enzyme sequences provided herein. See Mullis et al, U.S. Pat. No. 4,683,195; and Mullis, U.S. Pat. No. 4,683,202. The PCR reaction provides a method for selectively increasing the concentration of a particular nucleic acid sequence even when that sequence has not been previously purified and is present only in a single copy in a particular sample. The method can be used to amplify either single- or double-stranded DNA. The essence of the method involves the use of two oligonucleotide probes to serve as primers for the template-dependent, polymerase mediated replication of a desired nucleic acid molecule.

The recombinant DNA molecules of the present invention can be produced through any of a variety of means well known to the expert in the art and disclosed by, for example, Maniatis et al, supra. In order to replicate the KAT enzyme DNA sequences, these must be cloned in an appropriate vector. A vector is a replicable DNA construct. Vectors are used herein either to amplify DNA encoding the KAT enzyme and/or to express DNA which encodes the KAT enzyme. An expression vector is a replicable DNA construct in which a DNA sequence encoding the KAT enzyme is operably linked to suitable control sequences capable of effecting the expression of the KAT enzyme in a suitable host. DNA regions are operably linked when they are functionally related to each other. For example: a promoter is operably linked to a coding sequence if it controls the transcription of the sequence. Amplification vectors do not require expression control domains. All that is needed is the ability to replicate in a host, usually conferred by an origin of replication, and a selection gene to facilitate recognition of transformants.

DNA sequences encoding the KAT enzyme may be recombined with vector DNA in accordance with conventional techniques, including blunt-ended or staggered-ended termini for ligation, restriction enzyme digestion to provide appropriate termini, filling in of cohesive ends as appropriate, alkaline phosphatase treatment to avoid undesirable joining, and ligation with appropriate ligases. Techniques for such manipulation are disclosed by Maniatis et al, supra and are well known in the art.

Expression of the cloned sequence occurs when the expression vector is introduced into an appropriate host cell. If a prokaryotic expression vector is employed, then the appropriate host cell would be any prokaryotic cell capable of expressing the cloned sequences, for example E. coli. Similarly, if an eukaryotic expression vector is employed, then the appropriate host cell would be any eukaryotic cell capable of expressing the cloned sequence. A yeast host may be employed, for example S. cerevisiae. Alternatively, insect cells may be used, in which case a baculovirus vector system may be appropriate. Another alternative host is a mammalian cell line, for example COS-1 cells.

The need for control sequences into the expression vector will vary depending upon the host selected and the transformation method chosen. Generally, control sequences include a transcriptional promoter, an optional operator sequence to control transcription, a sequence encoding suitable mRNA ribosomal binding sites, and sequences which control the termination of transcription and translation. Vectors useful for practicing the present invention include plasmids, viruses (including phages), retroviruses, and integratable DNA fragments (i.e., fragments integratable into the host genome by homologous recombination). The vectors replicate and function independently of the host genome, or may, in some instances, integrate into the genome itself.

Expression vectors should contain a promoter which is recognized by the host organism. The promoter sequences of the present invention may be either prokaryotic, eukaryotic or viral. Example of suitable prokaryotic sequences include the P_(R) and P_(L) promoters of bacteriophage lambda (Hershey, The Bacteriophage Lambda, Ed., Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1973); and Hendrix, Lambda II, Ed., Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1980)); the trp, recA, heat shock, and lacZ promoters of E. coli and the SV40 early promoter. (Benoist et al, Nature, 290:304-310 (1981)).

As far as the Shine-Dalgarno sequence is concerned, preferred examples of suitable regulatory sequences are represented by the Shine-Dalgarno of the replicase gene of the phage MS-2 and of the gene cII of bacteriophage lambda. The Shine-Dalgarno sequence may be directly followed by the DNA encoding KAT and result in the expression of the mature KAT protein.

Alternatively, the DNA encoding KAT may be preceded by a DNA sequence encoding a carrier peptide sequence. In this case, a fusion protein is produced in which the N-terminus of KAT is fused to a carrier peptide, which may help to increase the protein expression levels and intracellular stability, and provide simple means of purification. A preferred carrier peptide includes one or more of the IgG binding domains of Staphylococcus protein A. Fusion proteins comprising IgG binding domains of protein A are easily purified to homogeneity by affinity chromatography, e.g., on IgG-coupled Sepharose. A DNA sequence encoding a recognition site for a proteolytic enzyme such as enterokinase, factor X or procollagenase may immediately precede the sequence for KAT to permit cleavage of the fusion protein to obtain the mature KAT protein.

Moreover, a suitable expression vector includes an appropriate marker which allows the screening of the transformed host cells. The transformation of the selected host is carried out using any one of the various techniques well known to the expert in the art and described in Maniatis et al, supra.

One further embodiment of the invention is a prokaryotic host cell transformed with the said expression vector and able to produce, under appropriate culture conditions, the KAT of the invention.

Cultures of cells derived from multicellular organisms are a desirable host for recombinant KAT synthesis. In principal, any eukaryotic cell culture is workable, whether from vertebrate or invertebrate culture, including insect cells. Propagation of such cells in cell culture has become a routine procedure. See Kruse et al, Tissue Culture, Eds., Academic Press (1973). Examples of useful host cell lines are HeLa cells, CHO and COS cell lines. The transcriptional and translational control sequences in expression vectors to be used in transforming vertebrate and invertebrate cells are often provided by viral sources. For example, commonly used promoters are derived from Adenovirus 2, polyoma and SV40. See, e.g. U.S. Pat. No. 4,599,308.

An origin of replication may be provided either by construction of the vector to include an exogenous origin or may be provided by the host cell chromosomal replication mechanism. If the vector is integrated into the host cell chromosome, the latter may be sufficient.

Rather than using vectors which contain viral origins of replication, one can transform mammalian cells by the method of cotransformation with a selectable marker and the KAT DNA. An example of a suitable marker is dihydrofolate reductase (DHFR) or thymidine kinase. See U.S. Pat. No. 4,399,216.

Cloned genes and vectors of the present invention are useful to transform cells which do not ordinarily express KAT to thereafter express this enzyme. Such cells are useful as intermediates for making recombinant KAT preparations useful for drug screening.

Moreover, genes and vectors of the present invention are useful in gene therapy. For such purposes, adenovirus vectors as well as retroviral vectors as described in Temin et al, U.S. Pat. No. 4,650,764 and Miller, U.S. Pat. No. 4,861,719 may be employed.

Cloned genes of the present invention, and oligonucleotides derived therefrom, are useful for screening for restriction fragment length polymorphism (RFLP) associated with certain disorders.

Oligonucleotides of the present invention are useful as diagnostic tools for probing KAT gene expression in various tissues. For example, tissue can be probed in situ with oligonucleotide probes carrying detectable groups by conventional autoradiography techniques to investigate native expression of this enzyme or pathological conditions relating thereto.

Genetically modified (transfected) cells have been successfully used for cerebral implantation. Cells transfected with the KAT gene can be useful for delivering kynurenic acid (or any other KAT product; see below) to the brain. This may prove to be an attractive means to circumvent the blood-brain barrier for kynurenic acid through peripheral administration of kynurenine (or any appropriate substrate of KAT; see below).

Transfected cells expressing large quantities of KAT are also useful for the production of neuroactive kynurenic analogs. For example, KAT is capable of forming the potent NMDA receptor antagonist and neuroprotectant 7-chlorokynurenic acid from its bioprecursor L-4-chlorokynurenine (J. Med. Chem., 37:334-336 (1994)).

The present invention is explained in greater detail in the following examples. These examples are intended to be illustrative of the present invention, and should not be constructed as limiting thereof.

EXAMPLE 1 Amino Acid Sequence of Tryptic Fragments of the Rat KAT

Protein Purification

Rat KAT was prepared essentially as described by Okuno et al, Brain Res., 534:37-44 (1990). The enzyme eluted from a Sephacryl S-200 column was separated by HPLC on a reverse-phase column (SC18, 250×4.6 mm, Japan Spectro. Co. Ltd). Elution was performed with a gradient of solvent A (70% vol/vol) acetonitrile in 0.1% trifluoroacetic acid (TFA)) and solvent B (0.1% TFA) applied for 40 min at a flow rate of 1 ml/min.

Trypsin and CNBr Digestion and Fragment Purification

500 pmoles of HPLC-purified rat KAT sample were digested by trypsin as described (Hugli, In: Techniques In Protein Chemistry, Eds., Academic Press, Inc., pages 377-391 (1989)) and by CNBr. These samples were subjected to reverse-phase HPLC after digestion and the resulting peaks collected.

Amino Acid Sequence Analysis

Sequence analysis was performed essentially as described (Fabbrini et al, FEBS Lett., 286:91-94 (1991)). FIG. 1 shows the partial amino acid sequence of rat KAT: N-terminus of mature KAT, (SEQ ID NO:14) a CNBr fragment (SEQ ID NO:15), tryptic fragment 112 of KAT (SEQ ID NO:16) and tryptic fragment 130 of KAT (SEQ ID NO:17).

EXAMPLE 2 Polymerase Chain Reaction (PCR) Cloning

RNA extraction

Total RNA from rat kidney was extracted from small quantities of tissue according to the instruction of RNAzol™ method (RNAzol-Cinna/Biotex Lab., Tex., U.S.A.).

First Strand cDNA Synthesis

First strand CDNA was synthesized from 3 mg of total RNA using 2 mg oligo polydT (18 pb), 4 ml of dNTP (2.5 mM), 8 ml of AMV buffer (TrisHCl pH8.8 250 mM/ KCl 200 mM/MgCl₂ 50 mM/ DTT 20 mM) in a final volume of 38.75 ml. The solution was boiled for 3 min at 65° C. and then placed on ice for 10 min; 0.75 ml of RNAsin (40 μ/ml Promega) and 0.5 ml of AMV Reverse transcriptase (25 μ/ml Boehringer Mannheim,GmbH, Germany) were added to the cold solution. The reaction was carried on at 42° C. for 2 h.

Design and Synthesis of Degenerated Oligonucleotides

Since the relative position of tryptic fragments 112 and 130 along the rat KAT primary structure was unknown, four degenerated oligonucleotides each 26 bp, were designed and synthesized using a DNA/RNA synthesizer (380B Applied Biosystems). The product of the reactions was purified on Sephadex G50 (Nap 25 Column, Pharmacia).

The sense orientation oligonucleotide, OligoA: (AAYYTNTGYCARCARCAYGAYGTNGT) (SEQ ID NO:20), and the anti-sense orientation oligonucleotide, OligoC: (ACNACRTCRTGYTGYTGRCANARRTT) (SEQ ID NO:21), were based on the peptide sequence Asn--Leu--Cys--Gln--Gln--His--Asp--Val--Val (residues 7-15 of fragment 130 (SEQ ID NO:17)). The sense orientation oligonucleotide, OligoB: (ACNGANARRTTYTGRTCXATNCCRTC) (SEQ ID NO:22), and the corresponding anti-sense oligonucleotide, OligoD: (GAYGGNATZGAYCARAAYYTNTCNGT) (SEQ ID NO:23), were based on the peptide sequence Asp--Gly--Ile--Asp--Gln--Asn--Leu--Ser--Val (residues 3-11 of fragment 112 (SEQ ID NO:16)) (N=T/C/A/G; Z=T/C/A; R=A/G; Y=T/C; X=T/G/A).

Polymerase Chain Reaction Condition

The first strand CDNA was divided in two aliquots and amplified by PCR as described below. The two oligonucleotide mixtures PCR1: oligoA and oligoD and PCR2: OligoB and OligoC were used as primers in the PCR reactions. 70 ng of template CDNA were combined with 10 mg of each set of primers, 10 ml of 10× Taq polymerase buffer (500 mM KCl/100 mM Tris--HCl, pH 8.3), 8 ml of 25 mM MgCl₂, 8 ml of a dNTP solution (2.5 mM dNTP) and 0.5 ml (2.5 units) of Taq DNA polymerase (Perkin Elmer Cetus). The volume was brought to 100 ml with H₂ O and the mixture was overlayed with mineral oil to prevent evaporation. The tube was heated to 94° C. for 3 min, denaturation was carried out for 3 minutes at 94° C., annealing for 2 min at 60° C. and polymerization for 2 min and 30 seconds at 72° C. The cycle was repeated 30 times.

A specific amplification product was observed only with PCR1. The product of the amplification was a DNA molecule of about 550 bp. The PCR1-amplification product was re-amplified using a new set of oligos, basically with the same sequence of oligoA and oligoc with SalI linkers and 5'-extra nucleotides. OligoE: (GCTAGTCGACACNACRTCRTGYTGYTGRCANARRTT) (SEQ ID NO:24) complementary to nucleotides coding for peptide 130 (SEQ ID NO:17) and OligoF: (GATCGTCGACGAYGGNATZGAYCARAAYYTNTCNGT) (SEQ ID NO:25) corresponding to nucleotides coding for peptide 112 (SEQ ID NO:16).

After PCR amplification, the resulting DNA fragment was digested overnight with the restriction enzyme SalI and ligated into the SalI site of the cloning plasmid pUC18 (Yanisch-Perron et al, Gene, 33:103-119 (1985)). The recombinant plasmid was extracted according to the instruction of the Qiagen Plasmid Maxi Protocol, precipitated with PEG, and denatured with NaOH 2 N.

Sequencing was carried out with universal and forward primers and subsequently with a series of synthetic oligonucleotide primers according to the dideoxy chain termination method (Sanger et al, Proc. Natl. Acad. Sci. USA, 74:5463-5467 (1977)) using Sequenase (United States Biochemicals Corp., Cleveland, Ohio).

Both strands of the insert were sequenced revealing an open reading frame of 196 amino acids. Part of the two rat KAT peptides that were sequenced are encoded by the corresponding 588 bp open reading frame. This open reading frame is used as probe in the cDNA library screening described in Example 3.

EXAMPLE 3 cDNA Library Screening

About 500,000 recombinant phages of λgt11 rat kidney CDNA library (Clontec Laboratories, USA) were plated on a lawn of E. coli Y1090 cells. After an overnight growth at 37° C. the recombinant phages were transferred to duplicate nitrocellulose filters; their DNA was then denatured, neutralized and baked under vacuum at 80° C. for 2 h. Prehybridization was carried out at 60° C. for 4 h in 6×SSC, 5× Denhardt's, 1% SDS, 200 μg/ml salmon sperm DNA. The filters were then hybridized overnight at 60° C. in the same mixture with the addition of about 1.5×10⁶ cpm/ml of labeled probe (see Example 2).

The probe was labeled with (³² p) dCTP by Multiprime DNA labeling system (Amersham), purified on Nick Column (Pharmacia) and added to the hybridizing solution.

The filters were washed at 60° C. twice in 2×SSC, 0.1% SDS and once in 1×SSC, 1% SDS. Filters were exposed to Kodak X-AR film (Eastman Kodak Company, Rochester, N.Y., USA) with intensifying screen at -80° C.

Positive phage plaques were isolated and screened again twice in order to isolate single clones.

Recombinant Phage DNA Extraction and Sequencing Methods

About 50,000 phages of each positive clone were plated on a lawn of E. coli Y1090 cells. After an overnight growth at 37° C., phages were resuspended in SM buffer (100 mM NaCl/8 mM MgSO₄ /50 mM Tris--HCl, pH 7.5/gelatin 0.001%) and chloroform 0.3%; the suspension was treated with 1 mg of RNAse and 1 mg of DNAse. Phage DNA was precipitated with PEG 10%/1 M NaCl, extracted with phenol and phenol:chloroform:iso-amyl alcohol and precipitated with PEG again.

The phage DNA was digested with EcoRI and the insert was ligated to the EcoRI site of pUC18.

The recombinant plasmid was extracted according to the instruction of Qiagen Plasmid Maxi Protocol; precipitated with PEG and denatured with 2 N NaOH.

Sequencing was carried out with universal and forward primers and subsequently with a series of synthetic oligonucleotide primers according to dideoxy chain termination method (Sanger et al, supra) using Sequenase (United States Biochemicals Corp., Cleveland, Ohio).

Three positive clones were isolated, cDNA-1, cDNA-2 and cDNA-3. Both strands of the three cDNAs were sequenced (see FIGS. 2A-2C, 3A-3D and 4A-4D).

cDNA-1 encodes a deduced protein of 423 amino acid residues, cDNA-2 encodes a deduced protein of 437 amino acid residues and cDNA-3 encodes a deduced protein of 457 amino acid residues.

The three deduced proteins differ only in their N-terminus. Moreover, the cDNA-2 and cDNA-3 clones are not homogeneous, since an alternative 5' sequence introduces an upstream ATG starting codon.

As already said, the longer proteins deduced from the cDNA-2 and cDNA-3 clones present a putative mitochondrial transit peptide in position 1 to 24 (cDNA-2) and in position 1 to 44 (cDNA-3) which is only partially present in the 423 amino acid protein.

EXAMPLE 4 Cloning of human KAT

A λ ZapII human brain CDNA library (Stratagene) was screened with a probe representing the N-terminal part of the cDNA-1, encompassing a sequence from amino acid residue 11 to 197 and encoding rat kidney KAT. About 1,350,000 recombinant phages were plated on a lawn of E. coli XL1 blue cells and screening was performed as described in the Example 3.

Positive phage plaques were isolated and screened again twice in order to isolate single clones.

Recombinant Phage DNA Extraction and Sequencing Methods

E. coli XL1 blue cells were coinfected with about 10⁵ phage particles corresponding to the positive clone selected and 1 μl of EX Assist helper phage (10⁶ pfu/ml). The mixture was incubated at 37° C. for 15 min and later incubated with 3 ml of LB for 3 h. Cells were spun down and the supernatant was heated 70° C. for 15 min. SORL cells at OD600=1 were mixed with the supernatant containing the phagemid pBluescript and incubated for 15 min at 37° C. and plated on LB-ampicillin plates (50 μg/ml). Single clones were incubated overnight in LB-ampicillin and DNA was extracted according to the instruction of the Qiagen Plasmid Maxi Protocol, then precipitated with PEG and denaturaed with NaOH 2 N. Sequencing was carried out with universal and forward primer and subsequently with a series of synthetic oligonucleotide primers according to the dideoxy chain termination method (Sanger et al, supra) using Sequenase (United States Biochemicals Corp., Cleveland, Ohio).

Unfortunately none of the positive clones contained a full length sequence. Therefore, in order to isolate the 5' missing sequence, a RACE protocol was performed.

5' PCR Race

0.5 μg of polyA+RNA from human brain was reverse transcribed with a primer (5'-CAGGGCCTGGAAGGCTGTGA-3') (SEQ ID NO:6) located at the N-terminal part of the longest cDNA clone isolated from the human brain cDNA library. Reaction was carried out as described in Example 2. 20 μl of the product was precipitated and resuspended in a mixture containing DATP 0.2 mM, buffer tailing (0.1 M potassium cacodylate pH 6.8, 1 mM CoCl₂, 100 mM DTT, 100 μg/ml BSA) and 15 U TdT enzyme (Gibco BRL). After incubation at 37° C. for 10 min, water was added to a final reaction volume of 250 μl. CDNA was mixed with 25 pmol of oligo (5'-ATAGCCACCAACAGTCACCA-3') (SEQ ID NO:7), 10 pmol of oligo (5'-GACTCGAGTCGACATCGATTTTTTTTTTTTTTTTT-3') (SEQ ID NO:8) and 25 pmol of oligo (5'-GACTCGAGTCGACATCGA-3') (SEQ ID NO:9), 10 μl of 10× Taq polymerase buffer (500 mM KCl/100 mM Tris--HCl, pH 8.3), 8 μl of 25 mM MgCl₂, 8 μl of a dNTP solution (2.5 mM dNTP). The volume was brought to 100 μl with H₂ O. The tube was heated at 95° C. for 7 min and 0.5 μl (2.5 U) of Taq polymerase (Perkin Elmer Cetus) were added. Annealing was carried out for 2 min at 58° C. and polymerization for 2.5 min at 72° C. The cycle was repeated 40 times. PCR products were blotted on a nitrocellulose filter and hybridized as described in Example 3 with a oligonucleotide probe (5'-ACCACTGACGAAGATCCTGGCAAGTTTCTTTGGGGAGC-3') (SEQ ID NO:10), based on the known sequence of the partial CDNA human clone. Probe was labeled with (λ³² p) dATP by T4 polynucleotide Kinase (Boehringer) and purified on a Nap5 column (Pharmacia). A positive band (330 bp), termed 5'-hKAT, was re-amplified using an oligo with SalI linkers then cloned in pUC18. DNA sequencing was performed on both strands confirming correspondence between the PCR fragment and the missing 5'-part of the human KAT clone.

EXAMPLE 5 Expression in Mammalian Cells

The expression plasmid encoding rat KAT was constructed as follows: to remove the 5' and the 3' untranslated sequences, as well as the putative mitochondrial targeting peptide, PCR amplification was performed using two specific oligonucleotides with XhoI linkers. The sense orientation oligonucleotide (5'-TGTCCTCGAGACCATGACCAAACGGCTGCAGGCTCGGA-3') (SEQ ID NO:26) begins at +241 of cDNA-1, whereas the antisense-orientation oligonucleotide (5'-GTACCTCGAGTCAGGGTTGGAGCTCTTTCCACTTG-3') (SEQ ID NO:27) complements the sequence starting from the end of the coding sequence. The XhoI-digested fragment, after being confirmed by sequencing, was cloned into the XhoI site of pSVL expression vector (Pharmacia Biotechnology).

The expression plasmid encoding human KAT was constructed as follows. In order to join the two cDNA fragments corresponding to the full length sequence of human KAT, two different PCR reactions were carried out. 5' hKAT was amplified by PCR using two specific oligonucleotides: a sense primer with XhoI linker (TGTCCTCGAGACCATGGCCAAACAGCTC) (SEQ ID NO:11) and as reverse primer (CAGGGCCTGGAAGGCTGTGA) (SEQ ID NO:6) the oligonucleotide used for the reverse transcription of Race (see Example 4). The partial CDNA sequence coding for human KAT obtained after cDNA library screening (Example 4) was PCR amplified using two primers flanking the cloning site: sense primer (GTAATACGACTCACTATAGGGC) (SEQ ID NO:12) and reverse primer (TGTCCTCGAGCGCTCTAGAACTAGTGGATC) (SEQ ID NO:13). The two PCR product were were digested with ApaI, linked together, digested XhoI and cloned into the PSVL vector. COS-1 cells were transfected with 10 μg of pSVL-ratKAT plasmid or pSVL-humanKAT by the calcium phosphate method (Maniatis et al, supra). 72 h after transfection, cells were disrupted by freezing and thawing, and after centrifugation, the supernatant was tested for KAT, glutamine transaminase K and cysteine conjugate β-lyase activities.

EXAMPLE 6 Kynurenine Amino Transferase, Glutamine Amino Transferase K and Cysteine Conjugate β-lyase Activities

Kynurenine transaminase assay

The reaction mixture (100 μl) contained 70 μM pyridoxal phosphate, 5 mM pyruvate, 3 mM kynurenine, and KAT sample in 0.17 M potassium phosphate buffer, pH 8.1, and was incubated at 37° C. for 1 h and 30 min. Reaction was stopped by adding 20 μl TCA 50% and the precipitate was removed by centrifugation. The supernatant was analyzed by HPLC with a C18 column (Vydac 201TP54, 25×4.6 cmxmm) at 1 ml/min, equilibrated with 5 mM acetic acid, 5% methanol, 0.1% heptane sulfonic acid, pH 3.0; kynurenic acid was eluted with 5OmM acetic acid, 5% methanol, 0.5% heptane sulfonic acid, pH 4.5. Absorbance at 243 nm was measured.

Glutamine Transaminase K Assay

Glutamine transaminase K activity was measured as described by Cooper and Meister (Methods Enzymol., 113:344-349 (1985)).

Cysteine Conjugate β-lyase Assay

The β-lyase assay was a coupled assay as described by Abraham and Cooper (1991). The product of the β-lyase reaction (pyruvate) was assayed by measuring the oxidation of NADH during the transformation of pyruvate to lactate catalyzed by alanine dehydrogenase. The reaction mixture (200 ml in a microtiter plate) contained 2 mM S-(1,2-dichlorovinyl)-L-cysteine (DCVC), 0.5 mM MTB, 0.1 mM PLP and the enzyme in 100 mM Tris buffer pH 8.8, and was incubated at 37° C. for 5, 10, 15 min prior the addition of 0.3 mM NADH, 7.3 U/ml alanine dehydrogenase, and ammonium acetate 0.1 M. Absorbance at 340 nm was measured using a microplate reader (Cerves uv900) and NADH concentration was calculated using a εl=4200 M⁻¹.

EXAMPLE 7 Amino Acid Sequence of Tryptic Fragments of the Human KAT

Human KAT was prepared essentially as described by Baran et al, J. Neurochem., 62:730-738 (1994).

500 pmoles of the purified human KAT sample were digested by trypsin as described (Hugli, In: Techniaues in Protein Chem., pages 377-391, Eds., Academic Press, Inc., (1989)). Briefly, human KAT was desalted using SMART system equipped with a Fast desalting column equilibrated in 10 mM ammonium bicarbonate. After the chromatography step, the sample was concentrated to a final volume of % ml. Cysteine residues in the molecule were reduced in 8 M urea, 10 mM DTT at 50° C. for 15 min then the alkylation was carried out with 20 mM iodoacetic acid for 15 min at room temperature. After this time the sample solution was diluted to have a final urea concentration of 2 M and the sample was digested overnight with trypsin (Boehringer) (enzyme:substrate ratio 1:25). Peptides resulting from digestion were analyzed by RP-HPLC using a Vydac C18 column and a linear gradient from 5 to 65% eluent B during 60 min, where eluent A was 0.1% trifluoroacetic acid (TFA) in water and eluent B was 0.07% TFA, 95% acetonitrile. Eluted peaks were manually collected, concentrated using a vacuum speedvac (Savant) and then loaded onto a 477 N-terminal protein sequencer (ABI, Perkin Elmer) for protein sequence determination.

Sequence analysis was performed essentially as described (Fabbrini et al, FEBS Lett., supra). FIG. 6 shows the amino acid sequence of three peptides of human KAT, namely F11 (SEQ ID NO:2), F13 (SEQ ID NO:3) and F14 (SEQ ID NO:4).

While the invention has been described in detail, and with reference to specific embodiments thereof, it will be apparent to one of ordinary skill in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.

    __________________________________________________________________________     #             SEQUENCE LISTING                                                    - -  - - (1) GENERAL INFORMATION:                                              - -    (iii) NUMBER OF SEQUENCES:  27                                          - -  - - (2) INFORMATION FOR SEQ ID NO: 1:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 1748 base - #pairs                                                 (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: cDNA                                               - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #1:                            - - CT TAATGTTTTT AGAGCTCACC ATG GCC AAA CAG CTG CAG - # GCC CGA AGG               49                                                                                         - #       Met Ala Lys Gln Leu Gln A - #la Arg Arg                              - #       1           - #    5                                - - CTA GAC GGG ATC GAC TAC AAC CCC TGG GTG GA - #G TTT GTG AAA CTG                - #94                                                                     Leu Asp Gly Ile Asp Tyr Asn Pro Trp Val Gl - #u Phe Val Lys Leu                10                  - #15                  - #20                                - - GCC AGT GAG CAT GAC GTC GTG AAC TTG GGC CA - #G GGC TTC CCG GAT               13 - #9                                                                    Ala Ser Glu His Asp Val Val Asn Leu Gly Gl - #n Gly Phe Pro Asp                25                  - #30                  - #35                                - - TTC CCA CCA CCA GAC TTT GCC GTG GAA GCC TT - #T CAG CAC GCT GTC               18 - #4                                                                    Phe Pro Pro Pro Asp Phe Ala Val Glu Ala Ph - #e Gln His Ala Val                40                  - #45                  - #50                                - - AGT GGA GAC TTC ATG CTT AAC CAG TAC ACC AA - #G ACA TTT GGT TAC               22 - #9                                                                    Ser Gly Asp Phe Met Leu Asn Gln Tyr Thr Ly - #s Thr Phe Gly Tyr                55                  - #60                  - #65                                - - CCA CCA CTG ACG AAG ATC CTG GCA AGT TTC TT - #T GGG GAG CTG CTG               27 - #4                                                                    Pro Pro Leu Thr Lys Ile Leu Ala Ser Phe Ph - #e Gly Glu Leu Leu                70                  - #75                  - #80                                - - GGT CAG GAG ATA GAC CCG CTC AGG AAT GTG CT - #G GTG ACT GTT GGT               31 - #9                                                                    Gly Gln Glu Ile Asp Pro Leu Arg Asn Val Le - #u Val Thr Val Gly                85                  - #90                  - #95                                - - GGC TAT GGG GCC CTG TTC ACA GCC TTC CAG GC - #C CTG GTG GAC GAA               36 - #4                                                                    Gly Tyr Gly Ala Leu Phe Thr Ala Phe Gln Al - #a Leu Val Asp Glu                100                 1 - #05                 1 - #10                             - - GGA GAC GAG GTC ATC ATC ATC GAA CCC TTT TT - #T GAC TGC TAC GAG               40 - #9                                                                    Gly Asp Glu Val Ile Ile Ile Glu Pro Phe Ph - #e Asp Cys Tyr Glu                115                 1 - #20                 1 - #25                             - - CCC ATG ACA ATG ATG GCA GGG GGT CGT CCT GT - #G TTT GTG TCC CTG               45 - #4                                                                    Pro Met Thr Met Met Ala Gly Gly Arg Pro Va - #l Phe Val Ser Leu                130                 1 - #35                 1 - #40                             - - AAG CCG GGT CCC ATC CAG AAT GGA GAA CTG GG - #T TCC AGC AGC AAC               49 - #9                                                                    Lys Pro Gly Pro Ile Gln Asn Gly Glu Leu Gl - #y Ser Ser Ser Asn                145                 1 - #50                 1 - #55                             - - TGG CAG CTG GAC CCC ATG GAG CTG GCC GGC AA - #A TTC ACA TCA CGC               54 - #4                                                                    Trp Gln Leu Asp Pro Met Glu Leu Ala Gly Ly - #s Phe Thr Ser Arg                160                 1 - #65                 1 - #70                             - - ACC AAA GCC CTG GTC CTC AAC ACC CCC AAC AA - #C CCC CTG GGC AAG               58 - #9                                                                    Thr Lys Ala Leu Val Leu Asn Thr Pro Asn As - #n Pro Leu Gly Lys                175                 1 - #80                 1 - #85                             - - GTG TTC TCC AGG GAA GAG CTG GAG CTG GTG GC - #C AGC CTT TGC CAG               63 - #4                                                                    Val Phe Ser Arg Glu Glu Leu Glu Leu Val Al - #a Ser Leu Cys Gln                190                 1 - #95                 2 - #00                             - - CAG CAT GAC GTG GTG TGT ATC ACT GAT GAA GT - #C TAC CAG TGG ATG               67 - #9                                                                    Gln His Asp Val Val Cys Ile Thr Asp Glu Va - #l Tyr Gln Trp Met                205                 2 - #10                 2 - #15                             - - GTC TAC GAC GGG CAC CAG CAC ATC AGC ATT GC - #C AGC CTC CCT GGC               72 - #4                                                                    Val Tyr Asp Gly His Gln His Ile Ser Ile Al - #a Ser Leu Pro Gly                220                 2 - #25                 2 - #30                             - - ATG TGG GAA CGG ACC CTG ACC ATC GGC AGC GC - #C GGC AAG ACC TTC               76 - #9                                                                    Met Trp Glu Arg Thr Leu Thr Ile Gly Ser Al - #a Gly Lys Thr Phe                235                 2 - #40                 2 - #45                             - - AGC GCC ACT GGC TGG AAG GTG GGC TGG GTC CT - #G GGT CCA GAT CAC               81 - #4                                                                    Ser Ala Thr Gly Trp Lys Val Gly Trp Val Le - #u Gly Pro Asp His                250                 2 - #55                 2 - #60                             - - ATC ATG AAG CAC CTG CGG ACC GTG CAC CAG AA - #C TCC GTC TTC CAC               85 - #9                                                                    Ile Met Lys His Leu Arg Thr Val His Gln As - #n Ser Val Phe His                265                 2 - #70                 2 - #75                             - - TGC CCC ACG CAG AGC CAG GCT GCA GTA GCC GA - #G AGC TTT GAA CGG               90 - #4                                                                    Cys Pro Thr Gln Ser Gln Ala Ala Val Ala Gl - #u Ser Phe Glu Arg                280                 2 - #85                 2 - #90                             - - GAG CAG CTG CTC TTC CGC CAA CCC AGC AGC TA - #C TTT GTG CAG TTC               94 - #9                                                                    Glu Gln Leu Leu Phe Arg Gln Pro Ser Ser Ty - #r Phe Val Gln Phe                295                 3 - #00                 3 - #05                             - - CCG CAG GCC ATG CAG CGC TGC CGT GAC CAC AT - #G ATA CGT AGC CTA               99 - #4                                                                    Pro Gln Ala Met Gln Arg Cys Arg Asp His Me - #t Ile Arg Ser Leu                310                 3 - #15                 3 - #20                             - - CAG TCA GTG GGC CTG AAG CCC ATC ATC CCT CA - #G GGC AGC TAC TTC              1039                                                                        Gln Ser Val Gly Leu Lys Pro Ile Ile Pro Gl - #n Gly Ser Tyr Phe                325                 3 - #30                 3 - #35                             - - CTC ATC ACA GAC ATC TCA GAC TTC AAG AGG AA - #G ATG CCT GAC TTG              1084                                                                        Leu Ile Thr Asp Ile Ser Asp Phe Lys Arg Ly - #s Met Pro Asp Leu                340                 3 - #45                 3 - #50                             - - CCT GGA GCT GTG GAT GAG CCC TAT GAC AGA CG - #C TTC GTC AAG TGG              1129                                                                        Pro Gly Ala Val Asp Glu Pro Tyr Asp Arg Ar - #g Phe Val Lys Trp                355                 3 - #60                 3 - #65                             - - ATG ATC AAG AAC AAG GGC TTG GTG GCC ATC CC - #T GTC TCC ATC TTC              1174                                                                        Met Ile Lys Asn Lys Gly Leu Val Ala Ile Pr - #o Val Ser Ile Phe                370                 3 - #75                 3 - #80                             - - TAT AGT GTG CCA CAT CAG AAG CAC TTT GAC CA - #C TAT ATC CGC TTC              1219                                                                        Tyr Ser Val Pro His Gln Lys His Phe Asp Hi - #s Tyr Ile Arg Phe                385                 3 - #90                 3 - #95                             - - TGT TTT GTG AAG GAT GAA GCC ACG CTC CAG GC - #C ATG GAC GAG AAG              1264                                                                        Cys Phe Val Lys Asp Glu Ala Thr Leu Gln Al - #a Met Asp Glu Lys                400                 4 - #05                 4 - #10                             - - CTG CGG AAG TGG AAG GTG GAA CTC TAGCCCTGAA GT - #CACGCCTT                    130 - #8                                                                    Leu Arg Lys Trp Lys Val Glu Leu                                                415                 4 - #20                                                     - - GGCCCTGACA TCCCCACATG CCCGCAGAGA TCCTCTTTGA GTGTCTGTCT  - #                 1358                                                                          - - TTGTCCAGGT TTCAGACATT TCTAGGTTGG GGAAGATGCT ATTGGGAAAC  - #                 1408                                                                          - - CTCTTCTCCG TGACACAGAA TGTTCTGGGT GGGAGCCGCC CTTCTTCATC  - #                 1458                                                                          - - TTAGAGAACC AAGTACCTCC TGTCTGAAAG GTGAGGGTGG CCTGACCTGG  - #                 1508                                                                          - - GCCTCTCCCT GCCCCTCCAT AGGTGGGTTT GTAGGGTCTT GTGTTGCTTC  - #                 1558                                                                          - - TGGTCTCTCC AGGCTTGGCT GAGACGGACG GTAGACTTCC ACCATGTACC  - #                 1608                                                                          - - GATCACATCC CAACTCTGCA TGGCCCCTGC TAAGGCTCAG GTATAACCTC  - #                 1658                                                                          - - ACCTTCCCTG GCTCATCTTG GCCTTGGGGA GTTGCCTTTA GGCTTGAGTC  - #                 1708                                                                          - - CTCAAGCCTC TCCTTTTCGT CCATAATAAA ATGGGAATTC     - #                       - #  1748                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO: 2:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 8 amino - #acids                                                   (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: peptide                                            - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #2:                            - - Thr Phe Ser Ala Thr Gly Xaa Lys                                           1               5                                                               - -  - - (2) INFORMATION FOR SEQ ID NO: 3:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 13 amino - #acids                                                  (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: peptide                                            - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #3:                            - - Ala Leu Val Leu Asn Thr Pro Asn Asn Pro Le - #u Gly Lys                   1               5   - #                10                                       - -  - - (2) INFORMATION FOR SEQ ID NO: 4:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 6 amino - #acids                                                   (B) TYPE: amino acid                                                           (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: peptide                                            - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #4:                            - - Glu Gln Leu Leu Phe Arg                                                   1               5                                                               - -  - - (2) INFORMATION FOR SEQ ID NO: 5:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 2101 base - #pairs                                                 (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: cDNA                                               - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #5:                            - - AAACTGACCA AGGAGTATGA TCAATCCCGT CCAGCCTCCG AGCCTGCAGC  - #                   50                                                                          - - CGTTTGGTCA TGGTGAGCTG CTTCAGCTAA CAATTGCACT GACAGTGCTC  - #                  100                                                                          - - TTGAGCCAAG TTGCTTCTGG GCGGAAGTAG TCCATCTAGG GCTCGGCCTC  - #                  150                                                                          - - TTTAAAGAAA CAGACTTCTG CAACCTTGGG ACTACGTTTG GGGTCGCCGG  - #                  200                                                                          - - CTATTGGACG GAGCAGCGCA ATTGTTAGCT GAAGCAGAAC TGTGTGTGGA  - #                  250                                                                          - - CTCAGGCCCT GGCTTGGAGC CATTTTCTGG GCTAGGCTGT CTGCCCTTCT  - #                  300                                                                          - - GTCCCTCTGG AGGGGAAGCC TGCAGTGCCT GTGGACCTAC CTCAGAGGCA  - #                  350                                                                          - - TGTTCAGGAG TGCAGCAGCC CTCTCGGTGC ACCTGATGTG GCCACTCTGG  - #                  400                                                                          - - GGAAGGAAAG CTGGAGCCTC ACTCACCCGG TGCTTGCACC AGTCTCTCAC  - #                  450                                                                          - - C ATG ACC AAA CGG CTG CAG GCT CGG AGG CTG - #GAC GGG ATT                   - #  490                                                                        Met Thr Lys Arg Leu Gln Ala Arg Arg L - #eu Asp Gly Ile                        1               5 - #                  - #10                                  - - GAT CAA AAC CTC TGG GTG GAG TTT GGC AAA CT - #G ACC AAG GAG                  - # 532                                                                     Asp Gln Asn Leu Trp Val Glu Phe Gly Lys Le - #u Thr Lys Glu                        15              - #    20              - #    25                            - - TAT GAC GTC GTG AAC TTG GGT CAG GGC TTC CC - #T GAC TTC TCG                  - # 574                                                                     Tyr Asp Val Val Asn Leu Gly Gln Gly Phe Pr - #o Asp Phe Ser                            30          - #        35          - #        40                        - - CCT CCG GAC TTT GCA ACG CAA GCT TTT CAG CA - #G GCT ACC AGT                  - # 616                                                                     Pro Pro Asp Phe Ala Thr Gln Ala Phe Gln Gl - #n Ala Thr Ser                                45      - #            50      - #            55                    - - GGG AAC TTC ATG CTC AAC CAG TAC ACC AGG GC - #A TTT GGT TAC                  - # 658                                                                     Gly Asn Phe Met Leu Asn Gln Tyr Thr Arg Al - #a Phe Gly Tyr                                    60  - #                65                                       - - CCA CCA CTG ACA AAC GTC CTG GCA AGT TTC TT - #T GGC AAG CTG                  - # 700                                                                     Pro Pro Leu Thr Asn Val Leu Ala Ser Phe Ph - #e Gly Lys Leu                    70                  - #75                  - #80                                - - CTG GGA CAG GAG ATG GAC CCA CTC ACG AAT GT - #G CTG GTG ACA                  - # 742                                                                     Leu Gly Gln Glu Met Asp Pro Leu Thr Asn Va - #l Leu Val Thr                        85              - #    90              - #    95                            - - GTG GGT GCC TAT GGG GCC TTG TTC ACA GCC TT - #T CAG GCC CTG                  - # 784                                                                     Val Gly Ala Tyr Gly Ala Leu Phe Thr Ala Ph - #e Gln Ala Leu                            100          - #       105          - #       110                       - - GTG GAT GAA GGA GAT GAG GTC ATC ATC ATG GA - #A CCT GCT TTT                  - # 826                                                                     Val Asp Glu Gly Asp Glu Val Ile Ile Met Gl - #u Pro Ala Phe                                115      - #           120      - #           125                   - - GAC TGT TAT GAA CCC ATG ACA ATG ATG GCT GG - #A GGT TGC CCT                  - # 868                                                                     Asp Cys Tyr Glu Pro Met Thr Met Met Ala Gl - #y Gly Cys Pro                                    130  - #               135                                      - - GTG TTC GTG ACT CTG AAG CCG AGC CCT GCT CC - #T AAG GGG AAA                  - # 910                                                                     Val Phe Val Thr Leu Lys Pro Ser Pro Ala Pr - #o Lys Gly Lys                    140                 1 - #45                 1 - #50                             - - CTG GGA GCC AGC AAT GAT TGG CAA CTG GAT CC - #T GCA GAA CTG                  - # 952                                                                     Leu Gly Ala Ser Asn Asp Trp Gln Leu Asp Pr - #o Ala Glu Leu                        155              - #   160              - #   165                           - - GCC AGC AAG TTC ACA CCT CGC ACC AAG GTC CT - #G GTC CTC AAC                  - # 994                                                                     Ala Ser Lys Phe Thr Pro Arg Thr Lys Val Le - #u Val Leu Asn                            170          - #       175          - #       180                       - - ACA CCC AAC AAC CCT TTA GGA AAG GTA TTC TC - #T AGG ATG GAG                  - #1036                                                                     Thr Pro Asn Asn Pro Leu Gly Lys Val Phe Se - #r Arg Met Glu                                185      - #           190      - #           195                   - - CTG GAG CTG GTG GCT AAT CTG TGC CAG CAG CA - #C GAT GTC GTG                  - #1078                                                                     Leu Glu Leu Val Ala Asn Leu Cys Gln Gln Hi - #s Asp Val Val                                    200  - #               205                                      - - TGC ATC TCT GAT GAG GTC TAC CAG TGG CTG GT - #C TAT GAC GGG                  - #1120                                                                     Cys Ile Ser Asp Glu Val Tyr Gln Trp Leu Va - #l Tyr Asp Gly                    210                 2 - #15                 2 - #20                             - - CAC CAG CAC GTC AGC ATC GCC AGC CTC CCT GG - #C ATG TGG GAT                  - #1162                                                                     His Gln His Val Ser Ile Ala Ser Leu Pro Gl - #y Met Trp Asp                        225              - #   230              - #   235                           - - CGG ACC CTG ACC ATC GGC AGT GCA GGC AAA AG - #C TTC AGT GCC                  - #1204                                                                     Arg Thr Leu Thr Ile Gly Ser Ala Gly Lys Se - #r Phe Ser Ala                            240          - #       245          - #       250                       - - ACT GGC TGG AAG GTG GGC TGG GTC ATG GGT CC - #A GAT AAC ATC                  - #1246                                                                     Thr Gly Trp Lys Val Gly Trp Val Met Gly Pr - #o Asp Asn Ile                                255      - #           260      - #           265                   - - ATG AAG CAC CTG AGG ACA GTG CAC CAG AAT TC - #T ATC TTC CAC                  - #1288                                                                     Met Lys His Leu Arg Thr Val His Gln Asn Se - #r Ile Phe His                                    270  - #               275                                      - - TGC CCC ACC CAG GCC CAG GCT GCA GTA GCC CA - #G TGC TTT GAG                  - #1330                                                                     Cys Pro Thr Gln Ala Gln Ala Ala Val Ala Gl - #n Cys Phe Glu                    280                 2 - #85                 2 - #90                             - - CGG GAG CAG CAA CAC TTT GGA CAA CCC AGC AG - #C TAC TTT TTG                  - #1372                                                                     Arg Glu Gln Gln His Phe Gly Gln Pro Ser Se - #r Tyr Phe Leu                        295              - #   300              - #   305                           - - CAG CTG CCA CAG GCC ATG GAG CTG AAC CGA GA - #C CAC ATG ATC                  - #1414                                                                     Gln Leu Pro Gln Ala Met Glu Leu Asn Arg As - #p His Met Ile                            310          - #       315          - #       320                       - - CGT AGC CTG CAG TCA GTG GGC CTC AAG CTC TG - #G ATC TCC CAG                  - #1456                                                                     Arg Ser Leu Gln Ser Val Gly Leu Lys Leu Tr - #p Ile Ser Gln                                325      - #           330      - #           335                   - - GGG AGC TAC TTC CTC ATT GCA GAC ATC TCA GA - #C TTC AAG AGC                  - #1498                                                                     Gly Ser Tyr Phe Leu Ile Ala Asp Ile Ser As - #p Phe Lys Ser                                    340  - #               345                                      - - AAG ATG CCT GAC CTG CCC GGA GCT GAG GAT GA - #G CCT TAT GAC                  - #1540                                                                     Lys Met Pro Asp Leu Pro Gly Ala Glu Asp Gl - #u Pro Tyr Asp                    350                 3 - #55                 3 - #60                             - - AGA CGC TTT GCC AAG TGG ATG ATC AAA AAC AT - #G GGC TTG GTG                  - #1582                                                                     Arg Arg Phe Ala Lys Trp Met Ile Lys Asn Me - #t Gly Leu Val                        365              - #   370              - #   375                           - - GGC ATC CCT GTC TCC ACA TTC TTC AGT CGG CC - #C CAT CAG AAG                  - #1624                                                                     Gly Ile Pro Val Ser Thr Phe Phe Ser Arg Pr - #o His Gln Lys                            380          - #       385          - #       390                       - - GAC TTT GAC CAC TAC ATC CGA TTC TGT TTT GT - #C AAG GAC AAG                  - #1666                                                                     Asp Phe Asp His Tyr Ile Arg Phe Cys Phe Va - #l Lys Asp Lys                                395      - #           400      - #           405                   - - GCC ACA CTC CAG GCC ATG GAT GAG AGA CTG CG - #C AAG TGG AAA                  - #1708                                                                     Ala Thr Leu Gln Ala Met Asp Glu Arg Leu Ar - #g Lys Trp Lys                                    410  - #               415                                      - - GAG CTC CAA CCC TGAGGAGGCT GCCCTCAGCC CCACCTCGAA  - #                       - #1750                                                                      Glu Leu Gln Pro                                                                420                                                                             - - CACAGGCCTC AGCTATGCCT TAGCACAGGG ATGGCACTGG AGGGCCCAGC  - #                 1800                                                                          - - TGTGTGACTG CGCATGTTTC CAGAAAAGAG GCCATGTCTT GGGGGTTGAA  - #                 1850                                                                          - - GCCATCCTTT CCCAGTGTCC ATCTGGACTA TTGGGTTGGG GGCCAGTTCT  - #                 1900                                                                          - - GGGTCTCAGC CTACTCCTCT GTAGGTTGCC TGTAGGGTTT TGATTGTTTC  - #                 1950                                                                          - - TGGCCTCTCT GCCTGGGGCA GGAAAGGGTG GAATATCAGG CCCGGTACCA  - #                 2000                                                                          - - CCTTAGCCCT GCCGAGGCTC TGTGGCTTCT CTACATCTTC TCCTGTGACC  - #                 2050                                                                          - - TCAGGATGTT GCTACTGTTC CTAATAAAGT TTTAAGTTAT TAGGACCCTC  - #                 2100                                                                          - - A                  - #                  - #                  - #                  2101                                                                    - -  - - (2) INFORMATION FOR SEQ ID NO: 6:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 20 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide primer"               - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #6:                            - - CAGGGCCTGG AAGGCTGTGA            - #                  - #                       - # 20                                                                    - -  - - (2) INFORMATION FOR SEQ ID NO: 7:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 20 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide"                      - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #7:                            - - ATAGCCACCA ACAGTCACCA            - #                  - #                       - # 20                                                                    - -  - - (2) INFORMATION FOR SEQ ID NO: 8:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 35 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide"                      - -    (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 8:                                - - GACTCGAGTC GACATCGATT TTTTTTTTTT TTTTT       - #                  -      #       35                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO: 9:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 18 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide"                      - -    (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 9:                                - - GACTCGAGTC GACATCGA             - #                  - #                       - #  18                                                                    - -  - - (2) INFORMATION FOR SEQ ID NO: 10:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 38 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide"                      - -    (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 10:                               - - ACCACTGACG AAGATCCTGG CAAGTTTCTT TGGGGAGC      - #                       - #     38                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO: 11:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 28 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide linker"               - -    (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 11:                               - - TGTCCTCGAG ACCATGGCCA AACAGCTC         - #                  - #                  28                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO: 12:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 22 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide primer"               - -    (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 12:                               - - GTAATACGAC TCACTATAGG GC           - #                  - #                      22                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO: 13:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH: 30 base - #pairs                                                   (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                  - -     (ii) MOLECULE TYPE: other nucleic acid                                          (A) DESCRIPTION:   / - #desc = "oligonucleotide primer"               - -    (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 13:                               - - TGTCCTCGAG CGCTCTAGAA CTAGTGGATC         - #                  - #                30                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:14:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  23 amin - #o acids                                                (B) TYPE:  amino aci - #d                                                      (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  peptide                                           - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #14:                          - - Leu Gln Ala Xaa Xaa Leu Asp Gly Ile Asp Gl - #n Asn                       1               5   - #                10                                       - - Leu Xaa Val Glu Phe Gly Lys Thr Xaa Glu Ty - #r                                   15          - #        20                                               - - (2) INFORMATION FOR SEQ ID NO:15:                                          - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  16 amin - #o acids                                                (B) TYPE:  amino aci - #d                                                      (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  peptide                                           - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #15:                          - - Xaa Xaa Leu Pro Gly Ala Glu Asp Gly Pro Ty - #r                           1               5   - #                10                                       - - Asp Arg Arg Xaa Ala                                                                   15                                                                  - - (2) INFORMATION FOR SEQ ID NO:16:                                          - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  14 amin - #o acids                                                (B) TYPE:  amino aci - #d                                                      (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  peptide                                           - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #16:                          - - Arg Leu Asp Gly Ile Asp Gln Asn Leu                                       1               5                                                               - - Ser Val Glu Phe Gly                                                       10                                                                              - - (2) INFORMATION FOR SEQ ID NO:17:                                          - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  31 amin - #o acids                                                (B) TYPE:  amino aci - #d                                                      (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  peptide                                           - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #17:                          - - Xaa Glu Leu Glu Leu Val Ala Asn Leu Cys Gl - #n Gln                       1               5   - #                10                                       - - His Asp Val Cys Ile Ser Asp Glu Val Tyr Gl - #n Gln                               15          - #        20                                               - - Val Tyr Asp Leu Gly His Gln                                               25                  - #30                                                       - - (2) INFORMATION FOR SEQ ID NO:18:                                          - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  1893 ba - #se pairs                                               (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA                                               - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #18:                          - - AAACTGACCA AGGAGTATGA TCAATCCCGT CCAGCCTCCG AGCCTGCAGC  - #                   50                                                                          - - CGTTTGGTCA TGGTGAGCTG CTTCAGCTAA CAATTGCACT GACAGTGCTC  - #                  100                                                                          - - TTGAGCCAAG TTGCTTCTGG GCGGAAGTAG TCCATCTAGG GCTCGGCCTC  - #                  150                                                                          - - TTTAAAGAAA CAGACTTCTG CAACCTTGGG ACTACGTTTG GGGTCGCCGG  - #                  200                                                                          - - CTATTGGACG GAGCAGCGCA ATTGTTAGCT GAAGCAGCTC ACC ATG AC - #C                   249                                                                        Met Thr                                                                        1                                                                               - - AAA CGG CTG CAG GCT CGG AGG CTG GAC GGG AT - #T GAT CAA AAC                  - # 291                                                                     Lys Arg Leu Gln Ala Arg Arg Leu Asp Gly Il - #e Asp Gln Asn                    5                  - # 10                 - # 15                                - - CTC TGG GTG GAG TTT GGC AAA CTG ACC AAG GA - #G TAT GAC GTC                  - # 333                                                                     Leu Trp Val Glu Phe Gly Lys Leu Thr Lys Gl - #u Tyr Asp Val                    20                  - #25                  - #30                                - - GTG AAC TTG GGT CAG GGC TTC CCT GAC TTC TC - #G CCT CCG GAC                  - # 375                                                                     Val Asn Leu Gly Gln Gly Phe Pro Asp Phe Se - #r Pro Pro Asp                    35                  - #40                                                       - - TTT GCA ACG CAA GCT TTT CAG CAG GCT ACC AG - #T GGG AAC TTC                  - # 417                                                                     Phe Ala Thr Gln Ala Phe Gln Gln Ala Thr Se - #r Gly Asn Phe                    45                  - #50                  - #55                                - - ATG CTC AAC CAG TAC ACC AGG GCA TTT GGT TA - #C CCA CCA CTG                  - # 459                                                                     Met Leu Asn Gln Tyr Thr Arg Ala Phe Gly Ty - #r Pro Pro Leu                    60                  - #65                  - #70                                - - ACA AAC GTC CTG GCA AGT TTC TTT GGC AAG CT - #G CTG GGA CAG                  - # 501                                                                     Thr Asn Val Leu Ala Ser Phe Phe Gly Lys Le - #u Leu Gly Gln                    75                  - #80                  - #85                                - - GAG ATG GAC CCA CTC ACG AAT GTG CTG GTG AC - #A GTG GGT GCC                  - # 543                                                                     Glu Met Asp Pro Leu Thr Asn Val Leu Val Th - #r Val Gly Ala                    90                  - #95                  - #100                               - - TAT GGG GCC TTG TTC ACA GCC TTT CAG GCC CT - #G GTG GAT GAA                  - # 585                                                                     Tyr Gly Ala Leu Phe Thr Ala Phe Gln Ala Le - #u Val Asp Glu                    105                 1 - #10                                                     - - GGA GAT GAG GTC ATC ATC ATG GAA CCT GCT TT - #T GAC TGT TAT                  - # 627                                                                     Gly Asp Glu Val Ile Ile Met Glu Pro Ala Ph - #e Asp Cys Tyr                    115                 1 - #20                 1 - #25                             - - GAA CCC ATG ACA ATG ATG GCT GGA GGT TGC CC - #T GTG TTC GTG                  - # 669                                                                     Glu Pro Met Thr Met Met Ala Gly Gly Cys Pr - #o Val Phe Val                    130                 1 - #35                 1 - #40                             - - ACT CTG AAG CCG AGC CCT GCT CCT AAG GGG AA - #A CTG GGA GCC                  - # 711                                                                     Thr Leu Lys Pro Ser Pro Ala Pro Lys Gly Ly - #s Leu Gly Ala                    145                 1 - #50                 1 - #55                             - - AGC AAT GAT TGG CAA CTG GAT CCT GCA GAA CT - #G GCC AGC AAG                  - # 753                                                                     Ser Asn Asp Trp Gln Leu Asp Pro Ala Glu Le - #u Ala Ser Lys                    160                 1 - #65                 1 - #70                             - - TTC ACA CCT CGC ACC AAG GTC CTG GTC CTC AA - #C ACA CCC AAC                  - # 795                                                                     Phe Thr Pro Arg Thr Lys Val Leu Val Leu As - #n Thr Pro Asn                    175                 1 - #80                                                     - - AAC CCT TTA GGA AAG GTA TTC TCT AGG ATG GA - #G CTG GAG CTG                  - # 837                                                                     Asn Pro Leu Gly Lys Val Phe Ser Arg Met Gl - #u Leu Glu Leu                    185                 1 - #90                 1 - #95                             - - GTG GCT AAT CTG TGC CAG CAG CAC GAT GTC GT - #G TGC ATC TCT                  - # 879                                                                     Val Ala Asn Leu Cys Gln Gln His Asp Val Va - #l Cys Ile Ser                    200                 2 - #05                 2 - #10                             - - GAT GAG GTC TAC CAG TGG CTG GTC TAT GAC GG - #G CAC CAG CAC                  - # 921                                                                     Asp Glu Val Tyr Gln Trp Leu Val Tyr Asp Gl - #y His Gln His                    215                 2 - #20                 2 - #25                             - - GTC AGC ATC GCC AGC CTC CCT GGC ATG TGG GA - #T CGG ACC CTG                  - # 963                                                                     Val Ser Ile Ala Ser Leu Pro Gly Met Trp As - #p Arg Thr Leu                    230                 2 - #35                 2 - #40                             - - ACC ATC GGC AGT GCA GGC AAA AGC TTC AGT GC - #C ACT GGC TGG                  - #1005                                                                     Thr Ile Gly Ser Ala Gly Lys Ser Phe Ser Al - #a Thr Gly Trp                    245                 2 - #50                                                     - - AAG GTG GGC TGG GTC ATG GGT CCA GAT AAC AT - #C ATG AAG CAC                  - #1047                                                                     Lys Val Gly Trp Val Met Gly Pro Asp Asn Il - #e Met Lys His                    255                 2 - #60                 2 - #65                             - - CTG AGG ACA GTG CAC CAG AAT TCT ATC TTC CA - #C TGC CCC ACC                  - #1089                                                                     Leu Arg Thr Val His Gln Asn Ser Ile Phe Hi - #s Cys Pro Thr                    270                 2 - #75                 2 - #80                             - - CAG GCC CAG GCT GCA GTA GCC CAG TGC TTT GA - #G CGG GAG CAG                  - #1131                                                                     Gln Ala Gln Ala Ala Val Ala Gln Cys Phe Gl - #u Arg Glu Gln                    285                 2 - #90                 2 - #95                             - - CAA CAC TTT GGA CAA CCC AGC AGC TAC TTT TT - #G CAG CTG CCA                  - #1173                                                                     Gln His Phe Gly Gln Pro Ser Ser Tyr Phe Le - #u Gln Leu Pro                    300                 3 - #05                 3 - #10                             - - CAG GCC ATG GAG CTG AAC CGA GAC CAC ATG AT - #C CGT AGC CTG                  - #1215                                                                     Gln Ala Met Glu Leu Asn Arg Asp His Met Il - #e Arg Ser Leu                    315                 3 - #20                                                     - - CAG TCA GTG GGC CTC AAG CTC TGG ATC TCC CA - #G GGG AGC TAC                  - #1257                                                                     Gln Ser Val Gly Leu Lys Leu Trp Ile Ser Gl - #n Gly Ser Tyr                    325                 3 - #30                 3 - #35                             - - TTC CTC ATT GCA GAC ATC TCA GAC TTC AAG AG - #C AAG ATG CCT                  - #1299                                                                     Phe Leu Ile Ala Asp Ile Ser Asp Phe Lys Se - #r Lys Met Pro                    340                 3 - #45                 3 - #50                             - - GAC CTG CCC GGA GCT GAG GAT GAG CCT TAT GA - #C AGA CGC TTT                  - #1341                                                                     Asp Leu Pro Gly Ala Glu Asp Glu Pro Tyr As - #p Arg Arg Phe                    355                 3 - #60                 3 - #65                             - - GCC AAG TGG ATG ATC AAA AAC ATG GGC TTG GT - #G GGC ATC CCT                  - #1383                                                                     Ala Lys Trp Met Ile Lys Asn Met Gly Leu Va - #l Gly Ile Pro                    370                 3 - #75                 3 - #80                             - - GTC TCC ACA TTC TTC AGT CGG CCC CAT CAG AA - #G GAC TTT GAC                  - #1425                                                                     Val Ser Thr Phe Phe Ser Arg Pro His Gln Ly - #s Asp Phe Asp                    385                 3 - #90                                                     - - CAC TAC ATC CGA TTC TGT TTT GTC AAG GAC AA - #G GCC ACA CTC                  - #1467                                                                     His Tyr Ile Arg Phe Cys Phe Val Lys Asp Ly - #s Ala Thr Leu                    395                 4 - #00                 4 - #05                             - - CAG GCC ATG GAT GAG AGA CTG CGC AAG TGG AA - #A GAG CTC CAA                  - #1509                                                                     Gln Ala Met Asp Glu Arg Leu Arg Lys Trp Ly - #s Glu Leu Gln                    410                 4 - #15                 4 - #20                             - - CCC TGAGGAGGCT GCCCTCAGCC CCACCTCGAA CACAGGCCTC AGCTATGCC - #T               1562                                                                        Pro                                                                             - - TAGCACAGGG ATGGCACTGG AGGGCCCAGC TGTGTGACTG CGCATGTTTC  - #                 1612                                                                          - - CAGAAAAGAG GCCATGTCTT GGGGGTTGAA GCCATCCTTT CCCAGTGTCC  - #                 1662                                                                          - - ATCTGGACTA TTGGGTTGGG GGCCAGTTCT GGGTCTCAGC CTACTCCTCT  - #                 1712                                                                          - - GTAGGTTGCC TGTAGGGTTT TGATTGTTTC TGGCCTCTCT GCCTGGGGCA  - #                 1762                                                                          - - GGAAAGGGTG GAATATCAGG CCCGGTACCA CCTTAGCCCT GCCGAGGCTC  - #                 1812                                                                          - - TGTGGCTTCT CTACATCTTC TCCTGTGACC TCAGGATGTT GCTACTGTTC  - #                 1862                                                                          - - CTAATAAAGT TTTAAGTTAT TAGGACCCTC A        - #                  - #             1893                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:19:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  2304 ba - #se pairs                                               (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA                                               - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #19:                          - - GGGCGACTCT AGATTTTTTT TTTTTTTTAC CTTCTACCTT TTATTGTCAC  - #                   50                                                                          - - GTGAACCATG GTCCTACAGG CTGCTGACAA GCTTGGCTGA GCAGGGATCC  - #                  100                                                                          - - CAGGGGCGTC GGCAGGAGAT GAGGAAGGGT TGCTGGGAGG GCTTGGCCTC  - #                  150                                                                          - - TTCCTTGAGA AGACAGCAAA TGTATCCAGC CTAGATTAAG GGTAGGGCAT  - #                  200                                                                          - - CCCCTATCCC TGTCAGTGGG CCTAGATCTC AGAGCCCCAC ATTAAAGACT  - #                  250                                                                          - - GCTAATGGGT CAGAAATGGG GGTCCCTTAG ATGGGGGTAG GCAGCAAGGC  - #                  300                                                                          - - CCTCCCTCCA GTGTTCTCAT TCTGTTCCGG TTTCATTTGT TGTGTCCAGG  - #                  350                                                                          - - GACGGTGAAG CAGATACCAG TCTCAAGCCC CAGGGTGCAG GAAGACGGGA  - #                  400                                                                          - - AATGGGAAAA TGGAAACATT CTTCAAGTGA CCAGAGCACT CTGCCGGGGA  - #                  450                                                                          - - CAAAAGACTT TGCCTTGAAC GCGTAGTGGA GAAGCTACAA ACCCCAGGTC  - #                  500                                                                          - - CCAGTGGCCT GATTGACTTA GGGTCTCAGC TGGCCCAAAA CTCAGTGTGT  - #                  550                                                                          - - AGATCAGACT GATCTCAAAC TCACAGAGAT CTCCCTGCCT TTGCCTGCTG  - #                  600                                                                          - - AGTCCTGGGA TTAAAGGC ATG AAT CAC AGT ACC TGG TGC - #CTT TTC                   645                                                                         Met Asn His Ser Thr Trp Cys Leu Phe                                            1               5                                                               - - TTT AAA AAG CTC ACC ATG ACC AAA CGG CTG CA - #G GCT CGG AGG                  - # 687                                                                     Phe Lys Lys Leu Thr Met Thr Lys Arg Leu Gl - #n Ala Arg Arg                    10                  - #15              20                                       - - CTG GAC GGG ATT GAT CAA AAC CTC TGG GTG GA - #G TTT GGC AAA                  - # 729                                                                     Leu Asp Gly Ile Asp Gln Asn Leu Trp Val Gl - #u Phe Gly Lys                    25                  - #30              35                                       - - CTG ACC AAG GAG TAT GAC GTC GTG AAC TTG GG - #T CAG GGC TTC                  - # 771                                                                     Leu Thr Lys Glu Tyr Asp Val Val Asn Leu Gl - #y Gln Gly Phe                    40                  - #45              50                                       - - CCT GAC TTC TCG CCT CCG GAC TTT GCA ACG CA - #A GCT TTT CAG                  - # 813                                                                     Pro Asp Phe Ser Pro Pro Asp Phe Ala Thr Gl - #n Ala Phe Gln                    55                  - #60              65                                       - - CAG GCT ACC AGT GGG AAC TTC ATG CTC AAC CA - #G TAC ACC AGG                  - # 855                                                                     Gln Ala Thr Ser Gly Asn Phe Met Leu Asn Gl - #n Tyr Thr Arg                    70                  - #75                                                       - - GCA TTT GGT TAC CCA CCA CTG ACA AAC GTC CT - #G GCA AGT TTC                  - # 897                                                                     Ala Phe Gly Tyr Pro Pro Leu Thr Asn Val Le - #u Ala Ser Phe                    80                  - #85                  - #90                                - - TTT GGC AAG CTG CTG GGA CAG GAG ATG GAC CC - #A CTC ACG AAT                  - # 939                                                                     Phe Gly Lys Leu Leu Gly Gln Glu Met Asp Pr - #o Leu Thr Asn                    95                  - #100                 - #105                               - - GTG CTG GTG ACA GTG GGT GCC TAT GGG GCC TT - #G TTC ACA GCC                  - # 981                                                                     Val Leu Val Thr Val Gly Ala Tyr Gly Ala Le - #u Phe Thr Ala                    110                 1 - #15                 1 - #20                             - - TTT CAG GCC CTG GTG GAT GAA GGA GAT GAG GT - #C ATC ATC ATG                  - #1023                                                                     Phe Gln Ala Leu Val Asp Glu Gly Asp Glu Va - #l Ile Ile Met                    125                 1 - #30                 1 - #35                             - - GAA CCT GCT TTT GAC TGT TAT GAA CCC ATG AC - #A ATG ATG GCT                  - #1065                                                                     Glu Pro Ala Phe Asp Cys Tyr Glu Pro Met Th - #r Met Met Ala                    140                 1 - #45                                                     - - GGA GGT TGC CCT GTG TTC GTG ACT CTG AAG CC - #G AGC CCT GCT                  - #1107                                                                     Gly Gly Cys Pro Val Phe Val Thr Leu Lys Pr - #o Ser Pro Ala                    150                 1 - #55                 1 - #60                             - - CCT AAG GGG AAA CTG GGA GCC AGC AAT GAT TG - #G CAA CTG GAT                  - #1149                                                                     Pro Lys Gly Lys Leu Gly Ala Ser Asn Asp Tr - #p Gln Leu Asp                    165                 1 - #70                 1 - #75                             - - CCT GCA GAA CTG GCC AGC AAG TTC ACA CCT CG - #C ACC AAG GTC                  - #1191                                                                     Pro Ala Glu Leu Ala Ser Lys Phe Thr Pro Ar - #g Thr Lys Val                    180                 1 - #85                 1 - #90                             - - CTG GTC CTC AAC ACA CCC AAC AAC CCT TTA GG - #A AAG GTA TTC                  - #1233                                                                     Leu Val Leu Asn Thr Pro Asn Asn Pro Leu Gl - #y Lys Val Phe                    195                 2 - #00                 2 - #05                             - - TCT AGG ATG GAG CTG GAG CTG GTG GCT AAT CT - #G TGC CAG CAG                  - #1275                                                                     Ser Arg Met Glu Leu Glu Leu Val Ala Asn Le - #u Cys Gln Gln                    210                 2 - #15                                                     - - CAC GAT GTC GTG TGC ATC TCT GAT GAG GTC TA - #C CAG TGG CTG                  - #1317                                                                     His Asp Val Val Cys Ile Ser Asp Glu Val Ty - #r Gln Trp Leu                    220                 2 - #25                 2 - #30                             - - GTC TAT GAC GGG CAC CAG CAC GTC AGC ATC GC - #C AGC CTC CCT                  - #1359                                                                     Val Try Asp Gly His Gln His Val Ser Ile Al - #a Ser Leu Pro                    235                 2 - #40                 2 - #45                             - - GGC ATG TGG GAT CGG ACC CTG ACC ATC GGC AG - #T GCA GGC AAA                  - #1401                                                                     Gly Met Trp Asp Arg Thr Leu Thr Ile Gly Se - #r Ala Gly Lys                    250                 2 - #55                 2 - #60                             - - AGC TTC AGT GCC ACT GGC TGG AAG GTG GGC TG - #G GTC ATG GGT                  - #1443                                                                     Ser Phe Ser Ala Thr Gly Trp Lys Val Gly Tr - #p Val Met Gly                    265                 2 - #70                 2 - #75                             - - CCA GAT AAC ATC ATG AAG CAC CTG AGG ACA GT - #G CAC CAG AAT                  - #1485                                                                     Pro Asp Asn Ile Met Lys His Leu Arg Thr Va - #l His Gln Asn                    280                 2 - #85                                                     - - TCT ATC TTC CAC TGC CCC ACC CAG GCC CAG GC - #T GCA GTA GCC                  - #1527                                                                     Ser Ile Phe His Cys Pro Thr Gln Ala Gln Al - #a Ala Val Ala                    290                 2 - #95                 3 - #00                             - - CAG TGC TTT GAG CGG GAG CAG CAA CAC TTT GG - #A CAA CCC AGC                  - #1569                                                                     Gln Cys Phe Glu Arg Glu Gln Gln His Phe Gl - #y Gln Pro Ser                    305                 3 - #10                 3 - #15                             - - AGC TAC TTT TTG CAG CTG CCA CAG GCC ATG GA - #G CTG AAC CGA                  - #1611                                                                     Ser Tyr Phe Leu Gln Leu Pro Gln Ala Met Gl - #u Leu Asn Arg                    320                 3 - #25                 3 - #30                             - - GAC CAC ATG ATC CGT AGC CTG CAG TCA GTG GG - #C CTC AAG CTC                  - #1653                                                                     Asp His Met Ile Arg Ser Leu Gln Ser Val Gl - #y Leu Lys Leu                    335                 3 - #40                 3 - #45                             - - TGG ATC TCC CAG GGG AGC TAC TTC CTC ATT GC - #A GAC ATC TCA                  - #1695                                                                     Trp Ile Ser Gln Gly Ser Tyr Phe Leu Ile Al - #a Asp Ile Ser                    350                 3 - #55                                                     - - GAC TTC AAG AGC AAG ATG CCT GAC CTG CCC GG - #A GCT GAG GAT                  - #1737                                                                     Asp Phe Lys Ser Lys Met Pro Asp Leu Pro Gl - #y Ala Glu Asp                    360                 3 - #65                 3 - #70                             - - GAG CCT TAT GAC AGA CGC TTT GCC AAG TGG AT - #G ATC AAA AAC                  - #1779                                                                     Glu Pro Tyr Asp Arg Arg Phe Ala Lys Trp Me - #t Ile Lys Asn                    375                 3 - #80                 3 - #85                             - - ATG GGC TTG GTG GGC ATC CCT GTC TCC ACA TT - #C TTC AGT CGG                  - #1821                                                                     Met Gly Leu Val Gly Ile Pro Val Ser Thr Ph - #e Phe Ser Arg                    390                 3 - #95                 4 - #00                             - - CCC CAT CAG AAG GAC TTT GAC CAC TAC ATC CG - #A TTC TGT TTT                  - #1863                                                                     Pro His Gln Lys Asp Phe Asp His Tyr Ile Ar - #g Phe Cys Phe                    405                 4 - #10                 4 - #15                             - - GTC AAG GAC AAG GCC ACA CTC CAG GCC ATG GA - #T GAG AGA CTG                  - #1905                                                                     Val Lys Asp Lys Ala Thr Leu Gln Ala Met As - #p Glu Arg Leu                    420                 4 - #25                                                     - - CGC AAG TGG AAA GAG CTC CAA CCC TGAGGAGGCT GC - #CCTCAGCC                    194 - #9                                                                    Arg Lys Trp Lys Glu Leu Gln Pro                                                430                 4 - #35                                                     - - CCACCTCGAA CACAGGCCTC AGCTATGCCT TAGCACAGGG ATGGCACTGG  - #                 1999                                                                          - - AGGGCCCAGC TGTGTGACTG CGCATGTTTC CAGAAAAGAG GCCATGTCTT  - #                 2049                                                                          - - GGGGGTTGAA GCCATCCTTT CCCAGTGTCC ATCTGGACTA TTGGGTTGGG  - #                 2099                                                                          - - GGCCAGTTCT GGGTCTCAGC CTACTCCTCT GTAGGTTGCC TGTAGGGTTT  - #                 2149                                                                          - - TGATTGTTTC TGGCCTCTCT GCCTGGGGCA GGAAAGGGTG GAATATCAGG  - #                 2199                                                                          - - CCCGGTACCA CCTTAGCCCT GCCGAGGCTC TGTGGCTTCT CTACATCTTC  - #                 2249                                                                          - - TCCTGTGACC TCAGGATGTT GCTACTGTTC CTAATAAAGT TTTAAGTTAT  - #                 2299                                                                          - - TAGGA                 - #                  - #                  - #               2304                                                                    - -  - - (2) INFORMATION FOR SEQ ID NO:20:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  26 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA (synthetic)                                   - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #20:                          - - AAYYTNTGYC ARCARCAYGA YGTNGT          - #                  - #                   26                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:21:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  26 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA (synthetic)                                   - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #21:                          - - ACNACRTCRT GYTGYTGRCA NARRTT          - #                  - #                   26                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:22:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  26 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA (synthetic)                                   - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #22:                          - - ACNGANARRT TYTGRTCDAT NCCRTC          - #                  - #                   26                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:23:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  26 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA (synthetic)                                   - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #23:                          - - GAYGGNATHG AYCARAAYYT NTCNGT          - #                  - #                   26                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:24:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  36 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA (synthetic)                                   - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #24:                          - - GCTAGTCGAC ACNACRTCRT GYTGYTGRCA NARRTT      - #                  -      #       36                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:25:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  36 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA (synthetic)                                   - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #25:                          - - GATCGTCGAC GAYGGNATHG AYCARAAYYT NTCNGT      - #                  -      #       36                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:26:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  38 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA (synthetic)                                   - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #26:                          - - TGTCCTCGAG ACCATGACCA AACGGCTGCA GGCTCGGA      - #                       - #     38                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO:27:                                     - -      (i) SEQUENCE CHARACTERISTICS:                                                  (A) LENGTH:  35 base - # pairs                                                 (B) TYPE:  nucleic a - #cid                                                    (C) STRANDEDNESS:  sing - #le                                                  (D) TOPOLOGY:  linear                                                 - -     (ii) MOLECULE TYPE:  DNA                                               - -     (xi) SEQUENCE DESCRIPTION:  SEQ ID NO: - #27:                          - - GTACCTCGAG TCAGGGTTGG AGCTCTTTCC ACTTG       - #                  -      #       35                                                                     __________________________________________________________________________ 

We claim:
 1. An isolated DNA sequence which encodes rat KAT enzyme, which comprises the sequence of the clone cDNA-1 (SEQ ID NO:18).
 2. An isolated DNA sequence which encodes rat KAT enzyme, which comprises the sequence of the clone cDNA-2 (SEQ ID NO:19).
 3. An isolated DNA sequence which encodes rat KAT enzyme, which comprises the sequence of the clone cDNA-3 (SEQ ID NO:5).
 4. A vector comprising a cloned DNA sequence as defined in any one of claims 1 to
 3. 5. A vector comprising a cloned DNA sequence as defined in any one of claims 1 to 3, wherein the vector is a plasmid.
 6. A vector comprising a cloned DNA sequence as defined in any one of claims 1 to 3, wherein the vector is a virus.
 7. A vector comprising a cloned DNA sequence as defined in any one of claims 3 to 5, wherein the vector is a retrovirus.
 8. A host cell transformed with a vector comprising a cloned DNA sequence as defined in any one of claims 3 to
 5. 9. A host cell transformed with a vector comprising a cloned DNA sequence as defined in any one of claims 3 to 5, wherein the cell is a mammalian cell.
 10. A method of producing neuroactive kynurenic analogs comprising transforming cells useful for producing neuroactive kynurenic analogs with a vector comprising a cloned DNA sequence as defined in any one of claims 1 to 3, growing transformed cells in media supplemented with a kynurenine analog, collecting the produce kynurenic analog produced by the said transformed cells, and testing said kynurenic analogs for neuroactive properties.
 11. A method of producing neuroactive kynurenic analogs comprising growing the host cell according to any one of claim 8 in media supplemented with a kynurenine analog, collecting said kynurenic analogs produced thereby, and testing said kynurenic analogs for neuroactive properties.
 12. A method of producing neuroactive kynurenic analogs comprising growing the host cell according to claim 9 in media supplemented with a kynurenine analog, collecting said kynurenic analogs produced thereby, and testing said kynurenic analogs for neuroactive properties. 